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510(k) clearance

Remex Spine Surgery Navigation - Universal Instruments

FDA 510(k) source

510(k) number
K262506
Applicant
Remex Medical Corp.
Decision date
Aug 20, 2026
Date received
Jul 21, 2026
Decision
Substantially Equivalent
Clearance type
Special
Product code
OLO
Device type
Orthopedic Stereotaxic Instrument
Device class
Class II
Regulation
21 CFR 882.4560
Advisory committee
Neurology
Statement or summary
Summary
Third party
N
Location
Taichung, TW